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Comment on “Is Acupuncture Effective in Diminishing Frown Lines? Evidence From a Randomized Controlled Trial” 《针灸能有效减少皱纹吗?》来自随机对照试验的证据”。
IF 2.5 4区 医学 Q2 DERMATOLOGY Pub Date : 2026-01-07 DOI: 10.1111/jocd.70663
Zihan Gao, Xiaoman Liu, Jiachun Xu

Haghir et al. conduct a pioneering randomized waitlist-controlled trial investigating the efficacy of combined facial and body acupuncture for frown lines, providing valuable evidence for this understudied cosmetic intervention [1]. The study demonstrates significant improvements in glabellar lines, patient satisfaction, and social functioning, with minimal adverse effects, supporting acupuncture as a safe alternative to invasive or toxin-based treatments.

However, several methodological considerations warrant attention. First, the control group was significantly younger than the intervention group (p = 0.03), a confounding factor given that younger age may inherently favor better skin condition and wrinkle improvement. Second, while outcome assessors and analysts were blinded, patients and the acupuncturist were not, introducing potential performance and expectation biases that could inflate efficacy outcomes. Third, the use of a wait-list control group does not account for placebo effects, which are particularly significant in nonpharmacological, perceptible interventions like acupuncture. The absence of a sham acupuncture control substantially limits the ability to attribute observed benefits specifically to the physiological effects of needling.

Controversially, the study attributes improvements to mechanisms like collagen synthesis and muscle relaxation but lacks objective measurements (skin elasticity, collagen density) to validate these biological claims, relying instead on subjective scales (GAIS, SSS). Additionally, the combined use of facial, body, and intradermal acupuncture prevents delineation of each component's specific contribution to outcomes.

Overall, this work advances evidence for acupuncture in facial rejuvenation, with strengths in blinded assessment and long-term follow-up. Addressing confounding variables, incorporating objective biometric measures, and testing component-specific effects in future multicenter trials will strengthen conclusions. Nevertheless, the study provides a compelling foundation for considering acupuncture as a safe, patient-centered option for frown line reduction.

All authors wrote the manuscript text. All authors have read and approved the final version of the manuscript.

The authors have nothing to report.

The authors have nothing to report.

The authors have nothing to report.

The authors declare no conflicts of interest.

Is acupuncture effective in diminishing frown lines? Evidence from a randomized controlled trial, https://doi.org/10.1111/jocd.70144.

The data that support the findings of this study are available on request from the corresponding author. The data are not publicly available due to privacy or ethical restrictions.

Haghir等人进行了一项开创性的随机候补对照试验,调查了面部和身体联合针灸治疗皱纹的疗效,为这种尚未得到充分研究的美容干预提供了有价值的证据[10]。该研究表明,在额骨线、患者满意度和社会功能方面有显著改善,副作用最小,支持针灸作为侵入性或基于毒素的治疗的安全替代方案。然而,有几个方法上的考虑值得注意。首先,对照组明显比干预组年轻(p = 0.03),考虑到年轻可能天生有利于更好的皮肤状况和皱纹改善,这是一个混淆因素。其次,虽然结果评估者和分析师是盲的,但患者和针灸师不是,这引入了可能夸大疗效结果的潜在表现和期望偏差。第三,等候名单对照组的使用并不能解释安慰剂效应,而安慰剂效应在针灸等非药物、可察觉的干预措施中尤为显著。缺乏假针灸对照,实质上限制了将观察到的益处具体归因于针刺的生理效应的能力。有争议的是,该研究将改善归因于胶原蛋白合成和肌肉松弛等机制,但缺乏客观测量(皮肤弹性、胶原蛋白密度)来验证这些生物学说法,而是依赖于主观量表(GAIS、SSS)。此外,面部、身体和皮内针灸的联合使用阻止了对每个组成部分对结果的具体贡献的描述。总的来说,这项工作提供了针灸面部年轻化的证据,在盲法评估和长期随访方面具有优势。在未来的多中心试验中,解决混杂变量、结合客观生物测量和测试组分特异性效应将加强结论。然而,这项研究提供了一个令人信服的基础,认为针灸是一种安全的,以患者为中心的减少皱纹的选择。所有作者都撰写了手稿文本。所有作者都阅读并认可了稿件的最终版本。作者没有什么可报告的。作者没有什么可报告的。作者没有什么可报告的。作者声明无利益冲突。针灸对减少皱纹有效吗?来自随机对照试验的证据,https://doi.org/10.1111/jocd.70144.The支持本研究结果的数据可根据通讯作者的要求获得。由于隐私或道德限制,这些数据不会公开。
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引用次数: 0
Auricular Acupuncture for Facial Aesthetics: A Preliminary Retrospective Clinical Study of 217 Cases 耳针面部美容217例临床初步回顾性研究。
IF 2.5 4区 医学 Q2 DERMATOLOGY Pub Date : 2026-01-07 DOI: 10.1111/jocd.70629
Wangpiaoyun Zhu, Panita Prateepjumraskul, Yike Han, Hantong Hu, Lifang Chen
<div> <section> <h3> Objective</h3> <p>In recent years, acupuncture has gained attention as a safe and natural method in cosmetic medicine. Auricular acupuncture has been insufficiently studied in the field of facial aesthetics. Our previous clinical observations were associated with rapid facial tightening, lifting, and slimming following auricular acupuncture, which is characterized by its simplicity, safety, and convenience.</p> </section> <section> <h3> Methods</h3> <p>In this retrospective study, we collected data from 242 participants who received auricular acupuncture for facial cosmetic treatment. Participants received weekly treatments, with facial photographs taken before and after each session. Outcome measures included the Wrinkle Severity Rating Scale (WSRS), Global Aesthetic Improvement Scale (GAIS), Visual Analogue Scale (VAS), and FACE-Q score. Evaluations were performed at three time points: before the first treatment, immediately after the first treatment, and following 3 months of continuous treatment. The safety assessment monitored adverse reactions during the trial period.</p> </section> <section> <h3> Results</h3> <p>A total of 217 participants were included in the statistical analysis as valid cases, of which 131 were assessed for immediate response and 86 for intermediate-term response. Immediate results showed a statistically significant decrease in WSRS scores (from 2.49 ± 0.69 to 1.86 ± 0.87, <i>p</i> < 0.05) and a 77.10% improvement in GAIS. Efficacy observation at 3 months showed WSRS score decreased from 2.53 ± 0.66 to 1.67 ± 0.73 (<i>p</i> < 0.05) and GAIS improvement of 95.35%. Participants reported high overall satisfaction with their facial appearance. After immediate treatment, the improvement in nasolabial folds was the most effective, with a score of 3.59 ± 0.62 (out of 5.00); after intermediate-term treatment, the improvement of the cheeks was the most effective, with a score of 3.78 ± 0.64 (out of 5.00). In both immediate and intermediate-term treatments, improvements were observed in the lower face and jawline, with relatively high satisfaction. Minimal pain was noted, with 64.98% reporting slight discomfort and 35.02% reporting no pain. No severe events were observed, affirming the treatment's safety and comfort.</p> </section> <section> <h3> Conclusions</h3> <p>Auricular acupuncture was associated with improvements in both immediate and intermediate-term evaluations. The immediate effects include facial slimming, lifting, reduction of nasolabial folds, and improvement of nasolabial lines. Intermediat
目的:近年来,针灸作为一种安全、自然的美容医学方法受到越来越多的关注。耳针在面部美学领域的研究还不够充分。我们之前的临床观察与耳针后面部快速收紧、提升和瘦身有关,其特点是简单、安全、方便。方法:在这项回顾性研究中,我们收集了242名接受耳针面部美容治疗的参与者的资料。参与者每周接受一次治疗,每次治疗前后都要拍摄面部照片。结果测量包括皱纹严重性评定量表(WSRS)、全球美学改善量表(GAIS)、视觉模拟量表(VAS)和FACE-Q评分。在三个时间点进行评估:第一次治疗前,第一次治疗后立即,连续治疗3个月后。安全性评估监测了试验期间的不良反应。结果:共有217例受试者作为有效病例纳入统计分析,其中131例为即时缓解,86例为中期缓解。即时结果显示,wrs评分从2.49±0.69降至1.86±0.87,p有统计学意义。结论:耳针与即时和中期评估的改善有关。直接效果包括面部瘦削,提高,减少鼻唇褶皱,改善鼻唇线。中期效果包括紧致面部、促进面部年轻化、整体面部增强和参与者满意度的提高。然而,鉴于作为回顾性研究的多重固有局限性,研究结果应被视为初步的,并应谨慎解释,未来的研究应采用前瞻性、充分有力的多中心设计,随访时间更长,验证患者报告的结果,标准化的图像采集,以及客观成像和生物力学指标的整合。
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引用次数: 0
Creation and Initial Validation of the Skin Dysmorphia Scale: Time for a New Concept to Arise in the Medical Field 皮肤畸形量表的创建和初步验证:医学领域出现新概念的时机。
IF 2.5 4区 医学 Q2 DERMATOLOGY Pub Date : 2026-01-05 DOI: 10.1111/jocd.70647
Feten Fekih-Romdhane, Rabih Hallit, Marita Hakim, Sahar Obeid, Diana Malaeb, Fouad Sakr, Mariam Dabbous, Frederic Harb, Souheil Hallit

Background

Skin dysmorphia is an emerging construct that reflects experiences of concern with perceived imperfections pertaining to skin coupled with an obsession with skincare routines to achieve flawless skin. It increasingly poses unique challenges to healthcare professionals and thus urgently necessitates a comprehensive approach to assessment and management. This study represents the first concerted effort to design and validate a psychometrically sound scale for use in clinical assessment and future research on skin dysmorphia that we called “Skin Dysmorphia Scale” (SDS).

Method

A cross-sectional survey was performed in July–August 2025 in Lebanon among adults from the general population.

Results

After removal of 11 items with significant cross-loadings, seven items remained which loaded onto a single factor and resulted in high internal consistency reliability (Cronbach's alpha = 0.83). A positive, moderate correlation was found between skin dysmorphia tendencies and general body dysmorphia symptoms, thereby supporting the convergent validity of the SDS. Heavier TikTok users showed significantly higher skin dysmorphia tendencies. Statistically significant correlations were observed between SDS scores and higher depression-anxiety symptoms. Moreover, skin dysmorphia symptoms were significantly and inversely correlated with self-esteem levels.

Conclusion

Preliminary analyses suggest that the newly developed SDS is a valid and reliable instrument for assessing skin dysmorphic concern and ensuring adequate, timely intervention or referral. We believe that it is timely and useful that skin dysmorphia be given high priority and be formally recognized by the medical and scientific community so that affected individuals can get the necessary medical or mental health care. Clinicians and researchers are encouraged to begin using the SDS in their practice.

背景:皮肤畸形是一种新兴的结构,反映了对与皮肤有关的感知缺陷的关注,以及对皮肤护理程序的痴迷,以达到完美的皮肤。它日益构成独特的挑战,医疗保健专业人员,因此迫切需要一个全面的方法来评估和管理。本研究首次共同设计并验证了一种心理测量学上健全的量表,用于临床评估和未来的皮肤畸形研究,我们称之为“皮肤畸形量表”(SDS)。方法:于2025年7月至8月在黎巴嫩的普通人群中进行了一项横断面调查。结果:在去除11个具有显著交叉加载的项目后,剩下7个项目被加载到单一因素上,具有较高的内部一致性信度(Cronbach’s alpha = 0.83)。发现皮肤畸形倾向与一般身体畸形症状呈正相关,从而支持SDS的收敛效度。重度抖音用户的皮肤畸形倾向明显更高。SDS评分与较高的抑郁焦虑症状之间存在统计学显著相关性。此外,皮肤畸形症状与自尊水平呈显著负相关。结论:初步分析表明,新开发的SDS是一种有效可靠的评估皮肤畸形的工具,可以确保充分、及时的干预或转诊。我们认为,医学界和科学界对皮肤畸形给予高度重视和正式承认,使受影响的个人能够得到必要的医疗或心理保健,这是及时而有益的。鼓励临床医生和研究人员在实践中开始使用SDS。
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引用次数: 0
A Topical Cosmeceutical Approach to Submental Fullness in Indian Women: 12-Week Prospective Study 局部药妆治疗印度女性精神饱满:12周的前瞻性研究。
IF 2.5 4区 医学 Q2 DERMATOLOGY Pub Date : 2026-01-05 DOI: 10.1111/jocd.70653
Subashini Selavdurairaj, Savitha Murali, Sivavallinathan Arunachalam, Ragavi Balasubramanian, C. Divyalakshmi, Vanathi Thirunavukkarasu, S. Anannya, Pavithra Sukumaran

Background

Submental fullness (“double chin”) is a common aesthetic concern among Indian women. No topical cosmeceutical has been systematically evaluated for this indication.

Objective

To assess the efficacy of a multi-active topical serum containing DMAE and retinol in reducing submental fullness in Indian women.

Methods

This 12-week, single-center, open-label study enrolled 16 women (ages 18–60) with mild-to-moderate submental fullness; 13 completed the trial. Subjects applied the serum nightly to the submental area. Standardized photographs were obtained at baseline and week 12 and were independently graded by two dermatologists using the validated Clinician-Reported Submental Fat Rating Scale. Any discordance was evaluated and resolved by a third, umpire dermatologist. Body weight was monitored throughout.

Results

All 13 completers showed visible improvement in submental contour. Dermatologist grading showed statistically significant improvements across all three views (p < 0.05), with the maximum change noted in the left and front profiles (r = 0.88 and 0.83, respectively) compared to the right profile (r = 0.61). Improvements were independent of body weight changes. No adverse events occurred.

Conclusion

This preliminary study demonstrates that a DMAE and retinol based topical serum can improve submental fullness in Indian women over 12 weeks, offering a noninvasive alternative to procedural interventions. Larger randomized controlled trials with objective volumetric endpoints are needed for validation.

背景:颏下丰满(“双下巴”)是印度女性普遍关注的审美问题。没有针对这一适应症的局部药妆被系统地评估过。目的:评价含有DMAE和视黄醇的多活性外用血清在减少印度妇女精神下丰满度方面的疗效。方法:这项为期12周、单中心、开放标签的研究招募了16名患有轻度至中度心理下丰满的女性(年龄18-60岁);13例完成试验。受试者每晚将血清涂抹在脑下区域。在基线和第12周获得标准化照片,并由两位皮肤科医生使用经过验证的临床医生报告的精神下脂肪评定量表独立评分。任何不一致都由第三位裁判员皮肤科医生评估和解决。整个过程中都监测了体重。结果:13名完成者的颏下轮廓均有明显改善。皮肤科医生的评分显示,三种观点均有统计学意义上的显著改善(p结论:本初步研究表明,DMAE和视黄醇局部血清可以在12周内改善印度妇女的颏下丰满度,为程序性干预提供了一种无创替代方案。需要更大规模的随机对照试验来验证客观体积终点。
{"title":"A Topical Cosmeceutical Approach to Submental Fullness in Indian Women: 12-Week Prospective Study","authors":"Subashini Selavdurairaj,&nbsp;Savitha Murali,&nbsp;Sivavallinathan Arunachalam,&nbsp;Ragavi Balasubramanian,&nbsp;C. Divyalakshmi,&nbsp;Vanathi Thirunavukkarasu,&nbsp;S. Anannya,&nbsp;Pavithra Sukumaran","doi":"10.1111/jocd.70653","DOIUrl":"10.1111/jocd.70653","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Background</h3>\u0000 \u0000 <p>Submental fullness (“double chin”) is a common aesthetic concern among Indian women. No topical cosmeceutical has been systematically evaluated for this indication.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Objective</h3>\u0000 \u0000 <p>To assess the efficacy of a multi-active topical serum containing DMAE and retinol in reducing submental fullness in Indian women.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>This 12-week, single-center, open-label study enrolled 16 women (ages 18–60) with mild-to-moderate submental fullness; 13 completed the trial. Subjects applied the serum nightly to the submental area. Standardized photographs were obtained at baseline and week 12 and were independently graded by two dermatologists using the validated Clinician-Reported Submental Fat Rating Scale. Any discordance was evaluated and resolved by a third, umpire dermatologist. Body weight was monitored throughout.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>All 13 completers showed visible improvement in submental contour. Dermatologist grading showed statistically significant improvements across all three views (<i>p</i> &lt; 0.05), with the maximum change noted in the left and front profiles (<i>r</i> = 0.88 and 0.83, respectively) compared to the right profile (<i>r</i> = 0.61). Improvements were independent of body weight changes. No adverse events occurred.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusion</h3>\u0000 \u0000 <p>This preliminary study demonstrates that a DMAE and retinol based topical serum can improve submental fullness in Indian women over 12 weeks, offering a noninvasive alternative to procedural interventions. Larger randomized controlled trials with objective volumetric endpoints are needed for validation.</p>\u0000 </section>\u0000 </div>","PeriodicalId":15546,"journal":{"name":"Journal of Cosmetic Dermatology","volume":"25 1","pages":""},"PeriodicalIF":2.5,"publicationDate":"2026-01-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/jocd.70653","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145900569","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Rapid and Visible Efficacy of a Dermocosmetic in Acne Patients With Fair Skin Phototypes: Results of a Randomized Split-Face Study 一种皮肤化妆品对白皙皮肤光型痤疮患者的快速和明显的疗效:一项随机裂脸研究的结果。
IF 2.5 4区 医学 Q2 DERMATOLOGY Pub Date : 2026-01-05 DOI: 10.1111/jocd.70641
Catherine Queille-Roussel, James Odeimi, Margot Broallier, Delphine Kerob, Jerry Tan

Introduction and Objectives

Dermocosmetics have proven their benefit in acne management. However, only very few studies investigated their efficacy kinetics. This study assessed the efficacy kinetics of a dermocosmetic cream (DC) containing Punica granatum Pericarp extract, Salicylic acid, Niacinamide, Zinc gluconate, and Aqua Posae Filiformis in subjects with acne.

Material and Methods

16 subjects (14 women, 2 men; mean age 29.4 ± 7.7 years; phototype II and III) with mild to moderate acne participated in a randomized, intra-individual, split-face study for 15 days. Hemi-faces randomly received DC or remained untreated. Assessments included lesion counts, acne severity, and local tolerance; subjects also rated the perceived benefit of the DC. Efficacy was also evaluated using standardized multi-modality full-face imaging and a mobile connected imaging system.

Results

The inflammatory lesion count significantly (p ≤ 0.05) decreased with DC at Day 8 and Day 15; a significant decrease of the non-inflammatory lesion count was observed at Day 15 (p < 0.01). The total lesion count had significantly (p ≤ 0.05) decreased with DC at Day 8 and Day 15. Between-side differences were significant (all p ≤ 0.05) for all lesion types at D15. Local tolerance was good. Most subjects considered that their skin appearance and the visibility of acne lesions had improved.

Conclusion

This exploratory study provides strong evidence on the efficacy kinetics of a DC cream in acne management in subjects with fair skin tones. It shows that early, daily and specific treatment with a targeted DC significantly improves all acne lesions type, as well as acne severity as soon as 15 days.

介绍和目的:皮肤化妆品已经证明了它们在痤疮管理方面的好处。然而,只有很少的研究调查了它们的疗效动力学。本研究评估了一种含有石榴果皮提取物、水杨酸、烟酰胺、葡萄糖酸锌和紫花水藻的护肤霜(DC)对痤疮患者的疗效动力学。材料与方法:16名轻至中度痤疮患者(女性14名,男性2名,平均年龄29.4±7.7岁,光型II和III型)参加了为期15天的随机、个体内、裂脸研究。半脸随机接受DC治疗或不接受治疗。评估包括病变计数、痤疮严重程度和局部耐受性;受试者还对DC的感知益处进行了评分。还使用标准化多模态全面成像和移动连接成像系统评估疗效。结果:第8天、第15天,随着DC的增加,炎症灶计数明显减少(p≤0.05);在第15天观察到非炎症性病变计数显著减少(p)结论:本探索性研究为DC霜在白皙肤色受试者痤疮管理中的功效动力学提供了强有力的证据。研究表明,早期、每日和有针对性的DC治疗可显著改善所有痤疮病变类型,并可在15天内改善痤疮严重程度。
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引用次数: 0
Prevalence of Acne and Its Impact on Quality of Life, Social Appearance Anxiety and Treatment Practices Among Young Adults 痤疮的患病率及其对年轻人生活质量、社交外貌焦虑和治疗方法的影响。
IF 2.5 4区 医学 Q2 DERMATOLOGY Pub Date : 2026-01-05 DOI: 10.1111/jocd.70654
Tajin Ahmed Jisa, Md. Tahalil Islam Rahat, Most. Shermin Akter Sumi, Nourin Sultana, Jibon Kumar Sarker, Mifta Nurejannath, Md. Kaderi Kibria
<div> <section> <h3> Background</h3> <p>Acne vulgaris is a common dermatological condition among young adults. It can cause psychosocial consequences that go beyond its physical effects.</p> </section> <section> <h3> Aims</h3> <p>This study aims to assess acne prevalence and its impact on quality of life, social appearance anxiety, and treatment practices among university students in northern Bangladesh.</p> </section> <section> <h3> Methods</h3> <p>A cross-sectional survey was conducted among 1067 students to assess acne prevalence and severity (Global Acne Grading System, GAGS). Quality of life, social appearance anxiety, and psychological distress were measured using the Dermatology Life Quality Index (DLQI), Social Appearance Anxiety Scale (SAAS), and Hospital Anxiety and Depression Scale (HADS). Sociodemographic, lifestyle, and familial factors were also evaluated. Descriptive statistics, chi-square tests, and binary logistic regression were used to identify significant associations and predictors.</p> </section> <section> <h3> Results</h3> <p>Acne was reported by 47.6% of participants. Among those affected (<i>n</i> = 465), 47.96% had mild acne, 44.95% had moderate acne, 6.02% had severe acne, and 1.08% had very severe acne. Increasing acne severity was significantly associated with poorer quality of life (<i>p</i> < 0.001) and higher social appearance anxiety (<i>p</i> = 0.013). Logistic regression identified several independent predictors of acne, including gender (<i>p</i> = 0.008), residence (<i>p</i> ≤ 0.033), middle-income status (<i>p</i> = 0.040), belief that diet affects acne (<i>p</i> < 0.001), smoking (<i>p</i> = 0.023), alcohol consumption (<i>p</i> = 0.001), and family history of acne (<i>p</i> < 0.001). Higher DLQI scores were also significantly associated with acne (<i>p</i> = 0.002), whereas SAAS and HADS were not independently associated. Among affected individuals, 33.7% consulted a dermatologist, while others relied on self-medication (29.9%), home remedies (30.8%), or combined approaches (23.7%).</p> </section> <section> <h3> Conclusions</h3> <p>Acne vulgaris is highly prevalent among young adults in northern Bangladesh and substantially impacts quality of life and social appearance. Its development involves a multifactorial interplay of genetic, lifestyle, and psychosocial factors, emphasizing the need for evidence-based management, lifestyle interventions, and psychosocial support in student health programs. Fut
背景:寻常痤疮是青壮年常见的皮肤病。它会造成超出身体影响的心理社会后果。目的:本研究旨在评估孟加拉国北部大学生的痤疮患病率及其对生活质量、社交外貌焦虑和治疗实践的影响。方法:对1067名学生进行横断面调查,评估痤疮的患病率和严重程度(全球痤疮分级系统,GAGS)。使用皮肤病生活质量指数(DLQI)、社会外表焦虑量表(SAAS)和医院焦虑抑郁量表(HADS)测量生活质量、社会外表焦虑和心理困扰。社会人口、生活方式和家庭因素也被评估。使用描述性统计、卡方检验和二元逻辑回归来确定显著关联和预测因素。结果:47.6%的参与者报告了痤疮。其中,轻度痤疮占47.96%,中度痤疮占44.95%,重度痤疮占6.02%,极重度痤疮占1.08%。痤疮严重程度的增加与较差的生活质量显著相关(p结论:寻常痤疮在孟加拉国北部的年轻人中非常普遍,并严重影响生活质量和社会形象。它的发展涉及遗传、生活方式和社会心理因素的多因素相互作用,强调在学生健康计划中需要循证管理、生活方式干预和社会心理支持。未来的研究应检查因果途径,并指导综合预防和治疗策略。
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引用次数: 0
Topical 4-Aminopyridine 5% in Male Androgenetic Alopecia: A Split-Scalp Exploratory Series 局部使用5%的4-氨基吡啶治疗男性雄激素性脱发:头皮分裂探索性系列。
IF 2.5 4区 医学 Q2 DERMATOLOGY Pub Date : 2026-01-04 DOI: 10.1111/jocd.70659
Nicolò Rivetti, Claudio Zeccara
<p>Androgenetic alopecia (AGA) is the most common form of hair loss in men, affecting up to 80% of individuals during their lifetime [<span>1</span>]. Current FDA-approved therapies, namely topical minoxidil and oral finasteride, can slow disease progression but do not induce de novo folliculogenesis [<span>1</span>]. Novel regenerative approaches are therefore of growing interest.</p><p>4-Aminopyridine (4-AP) is a voltage-gated potassium channel blocker approved for multiple sclerosis. In murine wound models, 4-AP has consistently promoted tissue regeneration: systemic administration accelerated closure and induced de novo folliculogenesis in excisional wounds [<span>2</span>], topical delivery improved burn healing with enhanced re-epithelialization and follicle formation [<span>3</span>], and systemic treatment further facilitated burn repair by modulating inflammation, apoptosis, angiogenesis, and extracellular matrix remodeling [<span>4</span>]. Based on this rationale, we conducted a split-scalp exploratory series to assess the potential of topical 4-AP 5% in men with AGA.</p><p>We included 10 male patients with AGA, mean age 35.8 years (range 22–49), Hamilton–Norwood stage I–V, who were recruited and followed from January 2025 to May 2025. All had been on stable topical and/or oral minoxidil for ≥ 12 months. Patients on finasteride or dutasteride were excluded. Each patient underwent eight sessions of microneedling (dermaroller 1.5 mm, passes until pinpoint bleeding) at 2-week intervals for 4 months. On the left scalp, 2 mL of a galenic 4-AP 5% solution was applied; on the right scalp, 2 mL of saline served as intra-patient control. Post-treatment care included betadine disinfection and avoidance of minoxidil for 24 h. Clinical efficacy was assessed at baseline and after 4 months using global photography and standardized trichoscopy at four fixed scalp sites (temporal angle, baihui acupoint, hair whorl, and occipital tuberosity), as described by Wang et al. [<span>5</span>], Trichoscan analysis (hair density, shaft diameter, terminal/vellus ratio), and pull test.</p><p>All 10 patients completed the study with topical 4-AP 5% solution, and no adverse events were reported. Global photography showed no visible improvement in density or hair caliber. Trichoscopy/Trichoscan revealed a mean hair density increase of +1.2 hairs/cm<sup>2</sup> on the 4-AP side vs. +0.8 hairs/cm<sup>2</sup> on the saline side (NS), with no significant changes in terminal-to-vellus hair ratio or mean shaft diameter. The pull test remained unchanged. Representative images from two patients are shown in Figure 1, while patient characteristics and outcomes are summarized in Table 1.</p><p>In our exploratory series, topical 4-AP 5% did not show measurable benefit in male AGA. Notably, the beneficial effects reported in animal studies were observed in the setting of skin wounds. In mice, 4-AP accelerated closure and induced de novo folliculogenesis in excisional wounds [<
雄激素性脱发(AGA)是男性中最常见的脱发形式,在其一生中影响多达80%的人。目前fda批准的治疗方法,即外用米诺地尔和口服非那雄胺,可以减缓疾病进展,但不会诱导新生卵泡发生。因此,新的再生方法日益引起人们的兴趣。4-氨基吡啶(4-AP)是一种批准用于多发性硬化症的电压门控钾通道阻滞剂。在小鼠伤口模型中,4- ap持续促进组织再生:全身给药加速切除伤口闭合并诱导新生卵泡形成[2],局部给药通过增强再上皮化和卵泡形成[3]改善烧伤愈合,全身治疗通过调节炎症、细胞凋亡、血管生成和细胞外基质重塑[4]进一步促进烧伤修复。基于这一基本原理,我们进行了一项头皮分离探索性系列研究,以评估5%外用4-AP治疗男性AGA的潜力。我们纳入10例男性AGA患者,平均年龄35.8岁(22-49岁),Hamilton-Norwood期I-V期,于2025年1月至2025年5月招募并随访。所有患者均稳定使用局部和/或口服米诺地尔≥12个月。排除非那雄胺或杜他雄胺的患者。每位患者每隔2周进行8次微针穿刺(穿刺1.5 mm,直至针尖出血),持续4个月。在左头皮上,应用2ml的益子酸4-AP 5%溶液;在右侧头皮上,2ml生理盐水作为患者内对照。治疗后护理包括氯他定消毒和避免使用米诺地尔24 h。临床疗效在基线和4个月后进行评估,根据Wang等人的描述,在四个固定的头皮部位(颞角、百会穴、发轮和枕粗隆)进行全像摄影和标准化毛镜检查,毛镜分析(头发密度、轴径、末端/绒毛比)和拉力试验。所有10例患者均使用局部4-AP 5%溶液完成研究,无不良事件报告。全球摄影显示密度和头发直径没有明显的改善。毛镜/毛扫描显示4-AP侧平均毛密度增加+1.2毛/cm2,而生理盐水侧(NS)平均毛密度增加+0.8毛/cm2,终末绒毛比或平均轴径无显著变化。拉力试验保持不变。两名患者的代表性图像如图1所示,患者特征和结局总结如表1所示。在我们的探索性系列研究中,局部4-AP 5%对男性AGA没有可测量的益处。值得注意的是,在动物研究中报告的有益效果是在皮肤伤口的情况下观察到的。在小鼠实验中,4- ap加速了切除伤口[2]的闭合和诱导新生卵泡形成,局部给药[3]时促进烧伤愈合和卵泡形成,全身给药[4]时通过调节炎症、凋亡、血管生成和细胞外基质重塑[4]增强烧伤修复。这些再生伤口愈合背景和雄激素驱动的AGA卵泡小型化之间的差异可能有助于解释为什么4-AP的效果没有转化为临床益处。因此,我们的研究结果强调了伤口愈合相关再生和雄激素性脱发之间的翻译差距,强调了从临床前模型到人类疾病的谨慎外推的必要性。这个探索性系列有几个限制。劈开头皮的设计,虽然允许患者内部比较,理论上可能允许有限的研究产品在治疗区域之间扩散。然而,4-氨基吡啶和盐水之间没有可测量的差异,这表明这种扩散对结果没有实质性影响。此外,在4个月的治疗期结束时评估疗效,没有延长治疗后随访,从而限制了对潜在延迟或长期影响的评估。最后,该研究的小样本量和探索性限制了这些发现的普遍性。在这个10例患者的裂头皮探索性系列研究中,局部4-氨基吡啶5%溶液联合微针治疗未能改善雄激素源性脱发的临床、皮肤镜或毛量测定参数。这些结果不支持在AGA中使用4-AP,至少在测试的配方和方案中是这样。Claudio Zeccara构思了这个想法并为研究设计做出了贡献。Nicolò Rivetti和Claudio Zeccara分别招募了5名患者,并参与了数据采集。Nicolò Rivetti起草了手稿。两位作者都对数据解释做出了贡献,对重要的知识内容进行了严格的修改,批准了最终版本,并同意对工作的各个方面负责。 所有患者均提供书面知情同意书,研究按照《赫尔辛基宣言》进行。鉴于这一试点经验的探索性和缺乏商业赞助,根据当地规定,不需要机构审查委员会的批准。已获得临床照片用于出版目的的书面知情同意。作者声明无利益冲突。支持本研究结果的数据可向通讯作者索取。由于隐私或道德限制,这些数据不会公开。
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引用次数: 0
Cosmetic Habits Associated With Breast Cancer in Benin: A Multicenter Case–Control Study 美容习惯与贝宁乳腺癌相关:一项多中心病例对照研究
IF 2.5 4区 医学 Q2 DERMATOLOGY Pub Date : 2026-01-02 DOI: 10.1111/jocd.70639
Dégboé Bérénice, Moutaïrou Gloria Moutaïrou, Gnangnon Fréddy, Ayinadou Marielle, Azon Kouanou Angèle, Zomalehto Zavier, Tonato Bagnan Angeline, Adégbidi Hugues, Atadokpèdé Félix

Introduction

Breast cancer remains the leading cause of cancer-related death among women worldwide. An increasing number of studies highlight the contribution of environmental and lifestyle factors, including cosmetic use, in its development.

Objective

To assess the association between cosmetic and dietary habits and breast cancer risk among women in Benin.

Methods

A case–control study was conducted involving 100 women diagnosed with breast cancer and matched 200 controls in the departments of visceral surgery, internal medicine, dermatology-venereology, and rheumatology at CNHU-HKM, and the gynecology-obstetrics department of CHU-MEL. Data were collected using a standardized questionnaire addressing family history, dietary patterns, and cosmetic product usage.

Results

In multivariate analysis, several cosmetic practices including the use of alkaline soaps (ORa = 7.26; p = 0.001), scented body lotions (ORa = 25.90; p < 0.001), perfumes (ORa = 30.43; p < 0.01), deodorants (ORa = 5.76; p = 0.009), shampoos/conditioners (ORa = 31.92; p < 0.001), and lipsticks (ORa = 69.12; p = 0.018) were significantly associated with increased breast cancer risk. First-degree family history of breast cancer was associated with more than a threefold increase in risk. Contrary to existing literature, the consumption of soy, beans, and sesame also appeared to be linked to a higher risk of breast cancer in this population.

Conclusion

Our results show a possible association between environmental factors—particularly the use of cosmetic products—and breast cancer. These results underscore a compelling need for a national cosmetovigilance system in Benin and public health initiatives promoting healthier lifestyles, especially among genetically predisposed women.

导读:乳腺癌仍然是全世界妇女癌症相关死亡的主要原因。越来越多的研究强调了环境和生活方式因素,包括化妆品的使用,在其发展中的作用。目的:评估贝宁妇女的化妆品和饮食习惯与乳腺癌风险之间的关系。方法:采用病例对照研究的方法,选取全国妇产医院内脏外科、内科、皮肤性病科、风湿科及朱美尔妇产科的100名确诊乳腺癌女性和200名对照患者。使用标准化问卷收集数据,包括家族史、饮食模式和化妆品使用情况。结果:在多因素分析中,使用碱性肥皂(ORa = 7.26, p = 0.001)、香味沐浴露(ORa = 25.90, p = 30.43, p = 5.76, p = 0.009)、洗发水/护发素(ORa = 31.92, p = 69.12, p = 0.018)与乳腺癌风险增加显著相关。有乳腺癌一级家族史的人患乳腺癌的风险增加了三倍以上。与现有文献相反,食用大豆、豆类和芝麻似乎也与这一人群患乳腺癌的风险增加有关。结论:我们的研究结果表明,环境因素——尤其是化妆品的使用——与乳腺癌之间可能存在关联。这些结果强调贝宁迫切需要建立一个全国化妆品警惕系统,并采取公共卫生举措,促进更健康的生活方式,特别是在遗传易感妇女中。
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引用次数: 0
A Real-Life Assessment of Injectable Polynucleotides High Purification Technology in Aesthetic Medicine for Skin Rejuvenation 可注射多核苷酸高纯化技术在皮肤年轻化美容医学中的应用。
IF 2.5 4区 医学 Q2 DERMATOLOGY Pub Date : 2026-01-02 DOI: 10.1111/jocd.70532
Lanza Eliana, Perna Anna, Bizzarri Stefania, Santoro Concetta, Cerutti Luisa, Dybala Agnieszka, Brunoro Andrea, Boffi Laura, Prussia Carolina, Saretta Simone

Background

Polynucleotides (PN) are innovative polymers that improve skin hydration and elasticity, serving as alternatives to traditional dermal fillers. Medical devices based on PN High Purification Technology (PN HPT) represent a new generation of injectable products designed to restore hydration, elasticity, and overall tissue quality. PN HPT is known for its clinical versatility and excellent tolerability.

Aims

To assess the real-world performance and safety of Plinest (40 mg/2 mL of PN HPT in a 2 mL pre-filled syringe), a CE-marked class III medical device for skin rejuvenation of the face, neck, and décolleté.

Methods

This observational clinical data collection involved 66 adult patients, each of whom could receive treatment in up to three areas (face, neck, décolleté). Patients underwent three sessions of intradermal PN HPT injections. A total of 106 questionnaires were collected: 47 for the face, 33 for the neck, and 26 for the décolleté. Performance was evaluated using the Global Clinical Improvement Scale (GCI-S) and Global Aesthetic Improvement Scale (GAIS). Safety was monitored through spontaneous adverse event (AE) reporting.

Results

Clinician-reported outcomes showed visible improvement in 100% of facial treatments, with 53.5% rated as “marked” or “excellent.” In the neck and décolleté areas, moderate to significant improvements were observed in over 93% and 88% of cases, respectively. Patient satisfaction ranged from 97% to 100%. No serious AEs occurred.

Conclusions

PN HPT demonstrated a favorable tolerability and performance profile in real-life aesthetic practice, supporting its role in improving skin quality and reducing signs of aging.

背景:多核苷酸(PN)是一种创新的聚合物,可以改善皮肤的水合作用和弹性,作为传统皮肤填充剂的替代品。基于PN高净化技术(PN HPT)的医疗设备代表了新一代可注射产品,旨在恢复水合作用,弹性和整体组织质量。PN HPT以其临床通用性和良好的耐受性而闻名。目的:评估Plinest (40mg / 2ml PN HPT在2ml预充注射器中)的实际性能和安全性,Plinest是一种ce标记的III类医疗器械,用于面部、颈部和颈部皮肤再生。方法:本观察性临床资料收集涉及66名成年患者,每位患者最多可接受三个区域(面部,颈部,颈部)的治疗。患者接受了三次皮内PN - HPT注射。总共收集了106份问卷:47份关于面部,33份关于颈部,26份关于臀部。使用全球临床改善量表(GCI-S)和全球美学改善量表(GAIS)评估其表现。通过自发不良事件(AE)报告来监测安全性。结果:临床医生报告的结果显示,100%的面部治疗都有明显的改善,其中53.5%被评为“显著”或“优秀”。在颈部和颈部,分别有超过93%和88%的病例有中度到显著的改善。患者满意度从97%到100%不等。未发生严重不良事件。结论:PN HPT在现实审美实践中表现出良好的耐受性和性能,支持其在改善皮肤质量和减少衰老迹象方面的作用。
{"title":"A Real-Life Assessment of Injectable Polynucleotides High Purification Technology in Aesthetic Medicine for Skin Rejuvenation","authors":"Lanza Eliana,&nbsp;Perna Anna,&nbsp;Bizzarri Stefania,&nbsp;Santoro Concetta,&nbsp;Cerutti Luisa,&nbsp;Dybala Agnieszka,&nbsp;Brunoro Andrea,&nbsp;Boffi Laura,&nbsp;Prussia Carolina,&nbsp;Saretta Simone","doi":"10.1111/jocd.70532","DOIUrl":"10.1111/jocd.70532","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Background</h3>\u0000 \u0000 <p>Polynucleotides (PN) are innovative polymers that improve skin hydration and elasticity, serving as alternatives to traditional dermal fillers. Medical devices based on PN High Purification Technology (PN HPT) represent a new generation of injectable products designed to restore hydration, elasticity, and overall tissue quality. PN HPT is known for its clinical versatility and excellent tolerability.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Aims</h3>\u0000 \u0000 <p>To assess the real-world performance and safety of Plinest (40 mg/2 mL of PN HPT in a 2 mL pre-filled syringe), a CE-marked class III medical device for skin rejuvenation of the face, neck, and décolleté.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>This observational clinical data collection involved 66 adult patients, each of whom could receive treatment in up to three areas (face, neck, décolleté). Patients underwent three sessions of intradermal PN HPT injections. A total of 106 questionnaires were collected: 47 for the face, 33 for the neck, and 26 for the décolleté. Performance was evaluated using the Global Clinical Improvement Scale (GCI-S) and Global Aesthetic Improvement Scale (GAIS). Safety was monitored through spontaneous adverse event (AE) reporting.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>Clinician-reported outcomes showed visible improvement in 100% of facial treatments, with 53.5% rated as “marked” or “excellent.” In the neck and décolleté areas, moderate to significant improvements were observed in over 93% and 88% of cases, respectively. Patient satisfaction ranged from 97% to 100%. No serious AEs occurred.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusions</h3>\u0000 \u0000 <p>PN HPT demonstrated a favorable tolerability and performance profile in real-life aesthetic practice, supporting its role in improving skin quality and reducing signs of aging.</p>\u0000 </section>\u0000 </div>","PeriodicalId":15546,"journal":{"name":"Journal of Cosmetic Dermatology","volume":"25 1","pages":""},"PeriodicalIF":2.5,"publicationDate":"2026-01-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12759169/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145892234","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Efficacy of Polynucleotide-Based Therapy in Atopic Dermatitis Management 多核苷酸治疗特应性皮炎的疗效观察。
IF 2.5 4区 医学 Q2 DERMATOLOGY Pub Date : 2026-01-02 DOI: 10.1111/jocd.70648
Kyungtae Bae, Youkyoung Cho, Kookjee Soo, Jeongwoo Lee, Youngjin Park, Yoonjeung Hyun, Jin-Hyun Kim, Kyuho Yi

Background

Atopic dermatitis (AD) is a chronic inflammatory skin disease characterized by persistent itching, dryness, redness, and recurrent eczematous lesions, significantly impacting patients' quality of life and psychological well-being. Despite various effective conventional treatments, innovative therapeutic approaches that simultaneously provide anti-inflammatory effects and enhanced skin hydration remain essential.

Objective

This case-series study aimed to evaluate the clinical efficacy, patient satisfaction, and safety profile of polynucleotide (PN)-based injectable therapies in patients with AD.

Methods

Patients with clinically diagnosed AD underwent intradermal injections of PN. Treatment outcomes were assessed by comparing standardized clinical photographs taken before and after the PN treatment, focusing on improvements in erythema, skin thickness, and overall skin hydration. Additionally, patient-reported outcomes, including reductions in itching, discomfort, and treatment satisfaction, were evaluated.

Results

Posttreatment evaluations demonstrated notable clinical improvements, including reduced erythema, decreased skin thickness, and enhanced skin hydration and elasticity. Patients consistently reported significant alleviation of itching and overall discomfort. Furthermore, high patient satisfaction and good adherence to treatment were observed, with no significant adverse events or side effects reported.

Conclusion

This exploratory case series provides preliminary observations suggesting that PN-based injectable therapies may offer benefits for patients with AD, particularly in improving skin hydration, barrier function, and symptomatic relief. While positive outcomes were documented in all four cases, the absence of validated scoring systems, objective biophysical measures, long-term follow-up, and a control group limits the strength and generalizability of these findings. PN injections in this context remain off-label, and further prospective, controlled studies with larger, more diverse populations are essential to establish efficacy, safety, optimal dosing regimens, and durability of response.

背景:特应性皮炎(AD)是一种慢性炎症性皮肤病,其特征为持续瘙痒、干燥、发红和反复发生的湿疹病变,严重影响患者的生活质量和心理健康。尽管有各种有效的传统治疗方法,同时提供抗炎作用和增强皮肤水合作用的创新治疗方法仍然是必不可少的。目的:本病例系列研究旨在评估基于多核苷酸(PN)的注射治疗在AD患者中的临床疗效、患者满意度和安全性。方法:临床诊断为AD的患者皮内注射PN。通过比较PN治疗前后拍摄的标准化临床照片来评估治疗结果,重点关注红斑、皮肤厚度和整体皮肤水化的改善。此外,还评估了患者报告的结果,包括瘙痒、不适和治疗满意度的减少。结果:治疗后评估显示显着的临床改善,包括红斑减少,皮肤厚度减少,皮肤水合性和弹性增强。患者一致报告瘙痒和整体不适的显著缓解。此外,观察到患者满意度高,治疗依从性好,无明显不良事件或副作用报告。结论:该探索性病例系列提供了初步观察结果,表明基于pn的注射疗法可能对AD患者有益,特别是在改善皮肤水合作用、屏障功能和症状缓解方面。虽然所有4例病例均记录了阳性结果,但缺乏有效的评分系统、客观的生物物理测量、长期随访和对照组限制了这些发现的强度和普遍性。在这种情况下,PN注射仍然是标签外的,进一步的前瞻性、对照研究,更大、更多样化的人群,对于确定有效性、安全性、最佳给药方案和反应的持久性至关重要。
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引用次数: 0
期刊
Journal of Cosmetic Dermatology
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